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Senior Medical Writer Ii

Propharma
Propharma
6+ years
Not Disclosed
Remote, India, India
10 May 6, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company Overview

ProPharma Group has over 20 years of experience improving patient health and wellness by supporting biotech, medical device, and pharmaceutical organizations.

Through its advise–build–operate model, ProPharma delivers end-to-end solutions across the product lifecycle, with expertise in:

  • Regulatory Sciences

  • Clinical Research Solutions

  • Quality & Compliance

  • Pharmacovigilance

  • Medical Information

  • R&D Technology


Role Title

Senior Medical Writer II (India)


Role Summary

The Senior Medical Writer II is responsible for authoring high-quality medical writing deliverables with a strong focus on accuracy, efficiency, and compliance. The role involves supporting ProPharma clients across clinical, regulatory, and safety documentation while collaborating with cross-functional teams.


Key Responsibilities

1. Medical Writing & Documentation

  • Author and edit a wide range of documents, including:

    • Protocols and protocol amendments

    • Clinical study reports (CSRs)

    • Patient narratives

    • Investigator’s Brochures (IBs)

    • Informed Consent Forms (ICFs)

    • Clinical Evaluation Plans/Reports (CEP/CER)

    • DSURs and plain language summaries

  • Develop complex regulatory documents:

    • PBRERs

    • IND, NDA, BLA, MAA submissions

    • eCTD submission-level documents


2. Regulatory Compliance

  • Ensure adherence to:

    • ICH E3 / ICH E6(R2) guidelines

    • EU MDR / IVDR regulations

    • Company SOPs and client standards

  • Maintain compliance with regulatory submission requirements and processes


3. Project & Client Management

  • Manage timelines and ensure deliverables are completed on time and within budget

  • Communicate directly with clients and manage expectations

  • Lead meetings such as:

    • Project kick-offs

    • Comment resolution discussions


4. Collaboration & Cross-functional Work

  • Work with:

    • Clinical Operations

    • Data Management

    • Biostatistics

    • Regulatory Affairs

  • Coordinate Quality Control (QC) reviews and maintain audit trails


5. Review & Quality Assurance

  • Review:

    • Statistical Analysis Plans (SAPs)

    • Tables, figures, and listings (TFLs)

  • Perform:

    • QC checks (e.g., validating tables vs. statistical outputs)

    • Peer reviews of documents


6. Team Leadership & Mentorship

  • Train, supervise, and mentor junior medical writers

  • Provide guidance on best practices and quality standards


7. Project Support & Administration

  • Manage deliverable trackers and timelines

  • Support internal and client meetings

  • Handle administrative tasks related to projects


8. Continuous Improvement

  • Stay updated on industry practices and regulatory guidelines

  • Identify inefficiencies and propose process improvements

  • Participate in departmental initiatives (e.g., training sessions, process enhancements)


Skills & Competencies

Technical & Domain Knowledge

  • Advanced knowledge of clinical research and data interpretation

  • Strong understanding of:

    • FDA and global regulatory requirements

    • Regulatory submission processes

Technical Skills

  • Advanced proficiency in:

    • MS Word (including tables, graphs, and formatting)

    • General computer and documentation tools

Core Competencies

  • Excellent project management skills

  • Strong written and verbal communication

  • High attention to detail and quality

  • Ability to manage multiple projects simultaneously

  • Strong collaboration and stakeholder management skills

  • Familiarity with AMA writing style

Behavioral Skills

  • Proactive and solution-oriented mindset

  • Strong organizational and time management skills

  • Ability to work independently and in teams

  • Growth mindset and adaptability


Education Requirements

  • Bachelor’s degree or higher in a medical or scientific discipline


Experience Requirements

  • Minimum 6+ years of experience in:

    • Clinical and/or regulatory medical writing

    • Drug, biologic, or medical device/diagnostic documentation

  • Experience in:

    • CROs

    • Pharmaceutical or biotechnology companies

  • Equivalent experience may be considered on a case-by-case basis


Work Environment

  • Remote work supported

  • Hybrid work encouraged for employees near office locations


Work Culture & Values

  • Commitment to Diversity, Equity & Inclusion

  • Equal Opportunity Employer

  • Encourages innovation, collaboration, and authenticity

  • Provides a supportive and inclusive workplace


Application Process

  • Applications are personally reviewed by the recruitment team

  • No AI-based screening is used

  • All applicants receive a response


Important Notice

  • No unsolicited resumes from recruiters or third parties

  • No phone calls or emails regarding this role